Home › Recall Archive › 2019 Recalls

Yearly recall archive

U.S. Recalls in 2019

Complete FDA and NHTSA recall records dated in 2019, organized for browsing by month, category and recalling company.

4,752recall records

4categories

12months represented

Dec 25, 2019latest record date

Monthly breakdown

2019 recalls by month

Select a month to review the recall records reported during that period.

December 2019321 records · 4 categories November 2019597 records · 4 categories October 2019525 records · 4 categories September 2019268 records · 4 categories August 2019505 records · 4 categories July 2019680 records · 4 categories June 2019445 records · 4 categories May 2019396 records · 4 categories April 2019242 records · 4 categories March 2019250 records · 4 categories February 2019381 records · 4 categories January 2019142 records · 4 categories

2019 recalls — page 42

Records are ordered by the best available source date.

VehicleOct 24, 2019

General Motors wheel speed sensor/tone ring recall — NHTSA campaign 19V761000

General Motors LLC (GM) is recalling certain 2015-2020 Chevrolet Suburban, Tahoe, and GMC Yukon, and 2014-2018 Chevrolet Silverado 1500 and GMC Sierra 1500 vehicles equipped with a…

wheel speed sensor/tone ringGeneral Motors LLC

Medical DeviceOct 23, 2019

Vital Scientific N.V Viva-E, Catalog # 6002-380, UDI # 03661540600050 Product Usage recall — FDA Z-0155-2020

The action was initiated due power supply failure. During a power supply failure the instruments malfunctions and no patient results are produced.

Class IIFDA: TerminatedVital Scientific N.V.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets recall — FDA Z-0137-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets recall — FDA Z-0129-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

Medical DeviceOct 23, 2019

Siemens Atellica CH 930 Analyzer recall — FDA Z-0148-2020

Atellica CH 930 Analyzer - Erroneous Indices for Hemolysis and Lipemia in Software versions 1.19.2 and below

Class IIFDA: TerminatedSiemens Healthcare Diagnostics, Inc.

Medical DeviceOct 23, 2019

Vital Scientific N.V Selectra ProM Analyzer, Catalog # 6003-435/UDI # 03661540600395 and recall — FDA Z-0157-2020

The action was initiated due power supply failure. During a power supply failure the instruments malfunctions and no patient results are produced.

Class IIFDA: TerminatedVital Scientific N.V.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets recall — FDA Z-0147-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets recall — FDA Z-0133-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

Medical DeviceOct 23, 2019

Roche Diagnostics Operations Cobas c Bilirubin Total Gen.3 recall — FDA Z-0153-2020

Due to low Quality Control recovery and invalid Calibration.

Class IIIFDA: TerminatedRoche Diagnostics Operations, Inc.

Medical DeviceOct 23, 2019

Vital Scientific N.V V-Twin, Catalog # 6002-800, UDI # 03661540600180 Product Usage recall — FDA Z-0156-2020

The action was initiated due power supply failure. During a power supply failure the instruments malfunctions and no patient results are produced.

Class IIFDA: TerminatedVital Scientific N.V.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets recall — FDA Z-0132-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

Medical DeviceOct 23, 2019

Vital Scientific N.V Selectra ProS Analyzer, Catalog # 6003-600/UDI # 03661540600418 Product recall — FDA Z-0158-2020

The action was initiated due power supply failure. During a power supply failure the instruments malfunctions and no patient results are produced.

Class IIFDA: TerminatedVital Scientific N.V.

Medical DeviceOct 23, 2019

Medtronic Vascular Galway DBA Medtronic Ireland Euphoria Rapid Exchange Balloon Dilatation recall — FDA Z-0122-2020

Medtronic has determined that some catheters have a slightly higher diameter stylette causing removal difficulties.

Class IIFDA: OngoingMedtronic Vascular Galway DBA Medtronic Ireland

Medical DeviceOct 23, 2019

OrthoPediatrics Adolescent attachment bolt used with the Pediatric Nailing Platform (PNP) recall — FDA Z-0125-2020

Interference can occur between the adolescent attachment bolt and the adolescent nail, cause a delay in surgical procedures

Class IIFDA: TerminatedOrthoPediatrics Corp

Medical DeviceOct 23, 2019

Vital Scientific N.V Viva - JR, catalog # 6002-940, UDI # 03661540600210 Product Usage recall — FDA Z-0154-2020

The action was initiated due power supply failure. During a power supply failure the instruments malfunctions and no patient results are produced.

Class IIFDA: TerminatedVital Scientific N.V.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets recall — FDA Z-0140-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets recall — FDA Z-0135-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets recall — FDA Z-0136-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets recall — FDA Z-0128-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets recall — FDA Z-0142-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

Medical DeviceOct 23, 2019

Roche Diagnostics cobas Integra Albumin Gen.2 recall — FDA Z-0152-2020

Due to low Quality Control recovery and invalid Calibration.

Class IIIFDA: TerminatedRoche Diagnostics Operations, Inc.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets recall — FDA Z-0138-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets recall — FDA Z-0126-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

Medical DeviceOct 23, 2019

ICU Medical Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets recall — FDA Z-0139-2020

Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.

Class IIFDA: TerminatedICU Medical Inc.

About the 2019 recall archive

This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.